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A mixture of routinely encountered xenobiotics induces both redox adaptations and perturbations in blood and tissues of rats after a long-term low-dose exposure regimen: The time and dose issue
dc.creator | Fountoucidou P., Veskoukis A.S., Kerasioti E., Docea A.O., Taitzoglou I.A., Liesivuori J., Tsatsakis A., Kouretas D. | en |
dc.date.accessioned | 2023-01-31T07:38:41Z | |
dc.date.available | 2023-01-31T07:38:41Z | |
dc.date.issued | 2019 | |
dc.identifier | 10.1016/j.toxlet.2019.09.015 | |
dc.identifier.issn | 03784274 | |
dc.identifier.uri | http://hdl.handle.net/11615/71741 | |
dc.description.abstract | Exposure of humans to xenobiotic mixtures is a continuous state during their everyday routine. However, the majority of toxicological studies assess the in vivo effects of individual substances rather than mixtures. Therefore, our main objective was to evaluate the impact of the 12- and 18-month exposure of rats to a mixture containing 13 pesticides, food, and life-style additives in three dosage levels (i.e. 0.0025 × NOAEL, 0.01 × NOAEL, and 0.05 × NOAEL), on redox biomarkers in blood and tissues. Our results indicate that the exposure to the mixture induces physiological adaptations by enhancing the blood antioxidant mechanism (i.e., increased glutathione, catalase and total antioxidant capacity and decreased protein carbonyls and TBARS) at 12 months of exposure. On the contrary, exposure to the 0.05 × NOAEL dose for 18 months induces significant perturbations in blood and tissue redox profile (i.e., increased carbonyls and TBARS). This study simulates a scenario of real-life risk exposure to mixtures of xenobiotics through a long-term low-dose administration regimen in rats. The results obtained could support, at least in part, the necessity of introducing testing of combined stimuli at reference doses and long term for the evaluation of the risk from exposure to chemicals. © 2019 Elsevier B.V. | en |
dc.language.iso | en | en |
dc.source | Toxicology Letters | en |
dc.source.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85072771349&doi=10.1016%2fj.toxlet.2019.09.015&partnerID=40&md5=60e02cf724a5360db503d08d90b227fa | |
dc.subject | catalase | en |
dc.subject | food preservative | en |
dc.subject | glutathione | en |
dc.subject | pesticide | en |
dc.subject | protein carbonyls | en |
dc.subject | thiobarbituric acid reactive substance | en |
dc.subject | unclassified drug | en |
dc.subject | xenobiotic agent | en |
dc.subject | biological marker | en |
dc.subject | catalase | en |
dc.subject | food additive | en |
dc.subject | glutathione | en |
dc.subject | thiobarbituric acid reactive substance | en |
dc.subject | xenobiotic agent | en |
dc.subject | animal experiment | en |
dc.subject | antioxidant assay | en |
dc.subject | Article | en |
dc.subject | blood | en |
dc.subject | brain | en |
dc.subject | controlled study | en |
dc.subject | erythrocyte concentrate | en |
dc.subject | female | en |
dc.subject | heart | en |
dc.subject | hemolysate | en |
dc.subject | kidney | en |
dc.subject | liver | en |
dc.subject | long term exposure | en |
dc.subject | lung | en |
dc.subject | male | en |
dc.subject | muscle | en |
dc.subject | no-observed-adverse-effect level | en |
dc.subject | nonhuman | en |
dc.subject | oxidative stress | en |
dc.subject | pancreas | en |
dc.subject | peroxidation | en |
dc.subject | priority journal | en |
dc.subject | protein carbonylation | en |
dc.subject | rat | en |
dc.subject | risk assessment | en |
dc.subject | spleen | en |
dc.subject | stomach | en |
dc.subject | tissue homogenate | en |
dc.subject | adverse event | en |
dc.subject | animal | en |
dc.subject | blood | en |
dc.subject | dose response | en |
dc.subject | drug effect | en |
dc.subject | environmental exposure | en |
dc.subject | metabolism | en |
dc.subject | oxidation reduction reaction | en |
dc.subject | oxidative stress | en |
dc.subject | risk assessment | en |
dc.subject | Sprague Dawley rat | en |
dc.subject | time factor | en |
dc.subject | Animals | en |
dc.subject | Biomarkers | en |
dc.subject | Catalase | en |
dc.subject | Dose-Response Relationship, Drug | en |
dc.subject | Environmental Exposure | en |
dc.subject | Female | en |
dc.subject | Food Additives | en |
dc.subject | Glutathione | en |
dc.subject | Male | en |
dc.subject | No-Observed-Adverse-Effect Level | en |
dc.subject | Oxidation-Reduction | en |
dc.subject | Oxidative Stress | en |
dc.subject | Pesticides | en |
dc.subject | Protein Carbonylation | en |
dc.subject | Rats, Sprague-Dawley | en |
dc.subject | Risk Assessment | en |
dc.subject | Thiobarbituric Acid Reactive Substances | en |
dc.subject | Time Factors | en |
dc.subject | Xenobiotics | en |
dc.subject | Elsevier Ireland Ltd | en |
dc.title | A mixture of routinely encountered xenobiotics induces both redox adaptations and perturbations in blood and tissues of rats after a long-term low-dose exposure regimen: The time and dose issue | en |
dc.type | journalArticle | en |
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